Truvic Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Truvic Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Symphony Thrombectomy System, Prodigy Thrombectomy System
2
Total
2
Cleared
0
Denied
Truvic Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Campbell, US.
Last cleared in 2023. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Truvic Medical, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Cardiomed Device Consultants and Cardiomed Devices Consultants.
FDA 510(k) Regulatory Record - Truvic Medical, Inc.
2 devices